20 Best senior scientist jobs in Cambridge, MA (Hiring Now!)

Site Manager-Dorchester, MA
Care Access —Dorchester, MA
Act as a primary point of contact in the therapeutic field for Care Access Research. Ability and willingness to mentor and guide less experienced CRC as they…
Estimated: $58.9K - $74.6K a year
Quick Apply
Health Economics & Outcomes Research Manager
Vertex Pharmaceuticals —Boston, MA
Minimum 4 years of experience in an HEOR department, or related field, in either an operational, project management or analytical role.
$134,400 - $201,600 a year
1d
MSAT Principal Scientist, Aseptic Control
Vertex Pharmaceuticals —Boston, MA
Work closely with colleagues in Process development to design and implement new technologies for aseptic filling of cell therapy drug products in novel device…
Estimated: $75.8K - $96K a year
Bench Scientist
Fortira Inc —Cambridge, MA
Transient cell culture techniques such as transfection, cell number and viability monitoring, cell lysis and protein harvest.
$30 - $35 an hour
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1d
Policy Advisor
Technical Assistance Collaborative —Boston, MA
Bachelor’s degree in a field related to the type of consultation TAC provides (social work, psychology, public health, or related health profession) required.
$100,000 a year
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Environmental Scientist - 24-196
Atlas Technical Consultants —Woburn, MA
Responsible for performing field data collection and sampling (soil, groundwater, soil vapor, and surface water), and office tasks (including field activity…
Estimated: $63.7K - $80.7K a year
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Wetland Scientist
Hancock Associates —Danvers, MA
Professional Wetland Scientist (PWS) license required. This role involves about 25% field work, 60% office work, and 15% conservation commission meeting…
$70,000 - $90,000 a year
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Life Science Field Support Technician
ChemoMetec Inc. —Somerville, MA
You will work with leading life science laboratories and companies, supporting them in the successful operation of their instrumentation.
Estimated: $41.8K - $52.9K a year
ELISA Developmental - Senior Scientist
Eurofins USA PSS Insourcing Solutions —Lexington, MA
You will be also authoring, reviewing and/or approving technical documents or regulatory filings ensuring high technical standards and compliance with…
Estimated: $93.4K - $118K a year
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1d
Applications Scientist - NMR
JEOL USA, Inc. —Peabody, MA
Extensive knowledge of liquids NMR applications and methods, knowledge of solid-state NMR a plus. Provide technical support to customers, sales, and marketing…
From $80,000 a year
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R&D Manager - New Markets
The Haartz Corporation —Acton, MA
Identify suitable raw materials and design appropriate constructions and manufacturing processes by understanding the basic performance requirements of the end…
Estimated: $79.2K - $100K a year
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4d
Senior Scientist, Analytical Development- Mutagenic Impurities
Vertex Pharmaceuticals —Boston, MA
Vertex is seeking a talented scientist eager to help develop both cutting-edge small molecule pharmaceuticals and the science underpinning the analytical…
Estimated: $75.1K - $95.1K a year
1d
Process Chemistry Senior Principal Scientist -Mutagenic Specialist
Vertex Pharmaceuticals —Boston, MA
Seek to employ state-of-the art technologies, including flow chemistry, photochemistry, electrochemistry, computational and predictive tools.
Estimated: $104K - $132K a year
Senior Environmental Scientist
AECOM —Boston, MA
Valid Driver's license is required. Bachelor's degree in science or related field. AECOM is the world’s trusted infrastructure consulting firm, delivering…
Estimated: $119K - $151K a year
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2d
Senior Environmental Engineer or Scientist
Integral Consulting Inc. —Boston, MA
Candidates should hold a B.S. or M.S. degree in hydrogeology, geology, environmental science, environmental or civil engineering, or related technical field;…
$105,000 - $165,000 a year
Process Chemistry Senior Principal Scientist
Vertex Pharmaceuticals —Boston, MA
The Sr. Principal Scientist Process Chemistry will lead/participate in cross-functional technical teams within their field of expertise.
Estimated: $104K - $132K a year
Laboratory Technician
Tailored Management —Burlington, MA
Bachelor’s Degree in a scientific field OR associate’s degree with 2+ years of related experience OR High School Diploma with 5+ years of related experience.
$22.64 - $29.20 an hour
Quick Apply
2d
Senior Scientist - ELISA
Eurofins USA PSS Insourcing Solutions —Lexington, MA
You will be also authoring, reviewing and/or approving technical documents or regulatory filings ensuring high technical standards and compliance with…
Estimated: $96.4K - $122K a year
Quick Apply
Service Technician for Flow Cytometer
Certified Genetool —Boston, MA
The Field Service Engineer is expected to proficiently troubleshoot, repair, and ensure optimal instrument performance while completing installations, repair,…
Estimated: $48.9K - $62K a year
Quick Apply
Senior Scientist, PK and Bioanalysis
Pharmaron —Woburn, MA
Ensure optimum performance of group Recommend and implement techniques to improve productivity, increase efficiencies, cut costs, take advantage of…
$85,000 - $110,000 a year
Quick Apply

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Site Manager-Dorchester, MA

Care Access - Dorchester, MA

Quick Apply

Job Details

Full-time Estimated: $58.9K - $74.6K a year

Benefits

Health savings account
Disability insurance
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Microsoft Word
Microsoft Excel
Clinical research
LVN
RN License
Phlebotomy
5 years
Writing skills
Research
IVR
Bachelor's degree
Clinical trials
Good Clinical Practice
Computer skills
LPN
Leadership
Communication skills
FDA regulations

Full Job Description

What We Do
Care Access is delivering the future of medicine today! Care Access has a revolutionary model that breaks down traditional barriers to clinical trials that limit participation among physicians and patients to 3%. By removing this bottleneck, Care Access is helping accelerate the approval and delivery of critical and life-saving therapies.

Who We Are
We care. Our people are the engines behind our mission: to revolutionize access to clinical trials for the benefit of patients everywhere. We care for one another, find new ideas to accelerate medicine, and seed a long-term impact for generations.

Position Overview
The Site Manager is responsible for the most pivotal and complex protocols and study designs being conducted at Care Access Research sites.

What You'll Be Working On

Duties include but not limited to:
Site Support Responsibilities:

Supports Key Sponsors and CROs
Manages some of the sites most challenging therapeutic areas and study designs
Able to monitor and mentor all levels of CRCs to ensure complete understanding of Care Access Research processes, SOPs and values, ensuring that a successful transition to more demanding opportunities and responsibilities
Assist Region Manager
Assist Region Manager in performing quality control check of all study source documents for completeness and quality

Therapeutic Responsibilities:

Demonstrate deep knowledge about the therapeutic area of responsibility
Demonstrate comprehensive understanding of related Protocol designs, outcomes and timelines
Engage in continuous independent learning within the therapeutic area of responsibility
Act as a primary point of contact in the therapeutic field for Care Access Research

Study Preparation:

Study Management:
Prioritize activities with specific regard to protocol timelines
Maintain adherence to FDA regulations and ICH guidelines in all aspects of conducting clinical trials.
Maintain effective relationships with study participants and other care Access Research personnel.
Interact in a positive, professional manner with patients, sponsor representatives, investigators and Care Access Research personnel and management.
Communicate clearly verbally and in writing.

Patient Coordination:
Prescreen study candidates
Obtain informed consent per Care Access Research SOP .
Complete visit procedures in accordance with protocol.
Train others and complete basic clinical procedures, such as blood draws, vital signs, ECGs, etc.
Review laboratory results, ECGs, and other test results (e.g., MRIs) for completeness and alert values, ensuring investigator review in a timely fashion.
Identify adverse events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor (where appropriate)

Documentation:
Record data legibly and enter in real time on paper or e-source documents
Accurately record study medication inventory, medication dispensation, and patient compliance.
Resolve data management queries and correct source data within sponsor provided timelines
Assist regulatory personnel with completion and filing of regulatory documents.
Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive.
Physical and Travel Requirements
This is an on-site position with regional commute requirements. Regularly planned travel within the region will be required as part of the role.

Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive

What You Bring
Role Requirements:

Knowledge, Skills and Abilities:

Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Understanding of issues affecting clinical research in the identified therapeutic area of expertise
Ability and willingness to mentor and guide less experienced CRC as they develop and gain experience in all therapeutic areas
Ability to communicate and work effectively with a diverse team of professionals
Excellent organizational, prioritization and leadership skills and capabilities with a strong attention to detail
Excellent computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
Critical thinker and problem solver
Excellent interpersonal skills, detailed oriented and meticulous
Friendly, outgoing personality with the ability to maintain a positive attitude under pressure
High level of self-motivation and energy
Excellent professional writing and communication skills
Ability to work independently in a fast-paced environment with minimal supervision

Certifications/Licenses, Education, and Experience:

RN or LPN/LVN preferred
Research Professional Certification- CRCC preferred
Bachelor’s Degree preferred, or equivalent combination of education, training and experience.
A minimum of 5 years experience as a Clinical Research Coordinator requied
Prefer1 year of experience as a Care Access Research Clinical Research Coordinator
Recent phlebotomy experience required

Benefits (US Full-Time Employees Only)

PTO/vacation days, sick days, holidays.
100% paid medical, dental, and vision Insurance. 75% for dependents.
HSA plan
Short-term disability, long-term disability, and life Insurance.
Culture of growth and equality
401k retirement plan

Diversity & Inclusion
We serve patients and researchers from diverse cultures and communities around the world. We are stronger and better when we build a team representing the people we aim to support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission. We value diversity and believe that unique contributions drive our success.
At Care Access, every day, we are advancing medical breakthroughs. We’re uniting standard patient care with cutting-edge treatments and research. Our work brings life-changing therapies to those in need and paves the way for newer and greater treatments to reach the world. We’re proud to advance these breakthroughs and work with the big players while engaging with the best
physicians and caring for patients. Our team of experts is paving the way to take this vision forward through innovation and a unique technology-enabled.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access currently is unable to sponsor work visas.

Job Type: Full-time

Quick Apply

senior scientist jobs in Cambridge, MA

Site Manager-Dorchester, MA

Health Economics & Outcomes Research Manager

MSAT Principal Scientist, Aseptic Control

Bench Scientist

Policy Advisor

Environmental Scientist - 24-196

Wetland Scientist

Life Science Field Support Technician

ELISA Developmental - Senior Scientist

Applications Scientist - NMR

R&D Manager - New Markets

Senior Scientist, Analytical Development- Mutagenic Impurities

Process Chemistry Senior Principal Scientist -Mutagenic Specialist

Senior Environmental Scientist

Senior Environmental Engineer or Scientist

Process Chemistry Senior Principal Scientist

Laboratory Technician

Senior Scientist - ELISA

Service Technician for Flow Cytometer

Senior Scientist, PK and Bioanalysis

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